Pazmiño N H, McEwan R, Ihle J N
J Exp Med. 1978 Nov 1;148(5):1338-50. doi: 10.1084/jem.148.5.1338.
The expression of terminal deoxynucleotidyl transferase (TdT) in the thymus and bone marrow of irradiated mice has been examined. Mice given the leukemogenic regimen of irradiation of four weekly doses of 175 rads starting at 1 mo of age show a long-term elimination of TdT activity in the bone marrow and a reduction of TdT activity in thymocytes. In such mice, the reappearance of normal levels of TdT in the thymus appears to only be associated with the onset of overt leukemia. This effect on TdT expression was shown to be uniquely associated with the leukemogenic regimen of irradiation in that nonleukemogenic irradiation or variations such as bone marrow reconstitution or age which reduce leukemias did not show the same phenotypic effects on TdT expression. The basis for the loss of TdT-positive cells was shown not to be due to the lack of the requisite factors involved in differentiation, but rather to the ability of leukemogenic doses of irradiation to reduce or eliminate an inducible bone marrow stem cell. These results are discussed with respect to the possible mechanisms involved in radiation-induced leukemias in mice.
已对受照射小鼠胸腺和骨髓中端粒脱氧核苷酸转移酶(TdT)的表达进行了检测。从1月龄开始每周接受4次、每次175拉德照射的诱变白血病照射方案的小鼠,其骨髓中TdT活性出现长期消除,胸腺细胞中TdT活性降低。在这类小鼠中,胸腺中TdT正常水平的重新出现似乎仅与明显白血病的发生有关。已表明这种对TdT表达的影响与诱变白血病照射方案有独特关联,因为非诱变白血病照射或诸如骨髓重建或年龄等可减少白血病发生的变化,对TdT表达并未表现出相同的表型效应。TdT阳性细胞丧失的基础并非由于缺乏参与分化的必要因子,而是由于诱变剂量的照射能够减少或消除可诱导的骨髓干细胞。针对小鼠辐射诱导白血病可能涉及的机制对这些结果进行了讨论。